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巴西副球孢子菌菌丝体阶段中CHS5和CHS4基因的转录水平,对外部渗透压、氧化应激和葡萄糖浓度的变化有反应。

Transcription levels of CHS5 and CHS4 genes in Paracoccidioides brasiliensis mycelial phase, respond to alterations in external osmolarity, oxidative stress and glucose concentration.

作者信息

Niño-Vega Gustavo A, Sorais Françoise, San-Blas Gioconda

机构信息

Instituto Venezolano de Investigaciones Científicas, Centro de Microbiología y Biología Celular, Apartado 20632, Caracas 1020A, Venezuela.

出版信息

Mycol Res. 2009 Oct;113(Pt 10):1091-6. doi: 10.1016/j.mycres.2009.07.005. Epub 2009 Jul 17.

DOI:10.1016/j.mycres.2009.07.005
PMID:19616626
Abstract

The complete sequence of Paracoccidioides brasiliensis CHS5 gene, encoding a putative chitin synthase revealed a 5583nt open reading frame, interrupted by three introns of 82, 87 and 97bp (GenBank Accession No EF654132). The deduced protein contains 1861 amino acids with a predicted molecular weight of 206.9kDa. Both its large size and the presence of a N-terminal region of approx. 800 residues with a characteristic putative myosin motor-like domain, allow us to include PbrChs5 into class V fungal chitin synthases. Sequence analysis of over 4kb from the 5' UTR region in CHS5, revealed the presence of a previously reported CHS4 gene in P. brasiliensis, arranged in a head-to-head configuration with CHS5. A motif search in this shared region showed the presence of stress response elements (STREs), three binding sites for the transcription activators Rlm1p (known to be stimulated by hypo-osmotic stress) and clusters of Adr1 (related to glucose repression). A quantitative RT-PCR analysis pointed to changes in transcription levels for both genes following oxidative stress, alteration of external osmolarity and under glucose-repressible conditions, suggesting a common regulatory mechanism of transcription.

摘要

巴西副球孢子菌CHS5基因的完整序列编码一种假定的几丁质合成酶,其开放阅读框为5583nt,被三个分别为82bp、87bp和97bp的内含子打断(GenBank登录号EF654132)。推导的蛋白质含有1861个氨基酸,预测分子量为206.9kDa。其较大的尺寸以及存在一个约800个残基的N端区域,该区域具有特征性的假定肌球蛋白运动样结构域,这使我们能够将PbrChs5归入V类真菌几丁质合成酶。对CHS5中5'UTR区域超过4kb的序列分析表明,巴西副球孢子菌中存在一个先前报道的CHS4基因,它与CHS5呈头对头排列。在这个共享区域进行的基序搜索显示存在应激反应元件(STREs)、转录激活因子Rlm1p的三个结合位点(已知受低渗应激刺激)以及Adr1簇(与葡萄糖阻遏相关)。定量RT-PCR分析表明,在氧化应激、外部渗透压改变和葡萄糖可阻遏条件下,这两个基因的转录水平均发生变化,提示存在共同的转录调控机制。

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